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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Socs1tm1Jni
targeted mutation 1, James N Ihle
MGI:3051623
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Socs1tm1Jni/Socs1tm1Jni Not Specified MGI:3051903
ht2
Socs1tm1Jni/Socs1+ Not Specified MGI:3051904
cx3
Ifngtm1Ts/Ifngtm1Ts
Socs1tm1Jni/Socs1tm1Jni
involves: 129S7/SvEvBrd MGI:3783715


Genotype
MGI:3051903
hm1
Allelic
Composition
Socs1tm1Jni/Socs1tm1Jni
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Socs1tm1Jni mutation (0 available); any Socs1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes die by 3 weeks of age

hematopoietic system
• numbers begin to decrease within a few days of birth
• by day 10 an almost exclusively single positive population of cells
• significant numbers of CD4+ and CD8+ cells in bone marrow
• peripheral splenic T cells are morphologically large blasting cells
• T-cells proliferate in response to Il-2 alone
• dramatically reduced numbers of B cells in the spleen

immune system
• numbers begin to decrease within a few days of birth
• by day 10 an almost exclusively single positive population of cells
• significant numbers of CD4+ and CD8+ cells in bone marrow
• peripheral splenic T cells are morphologically large blasting cells
• T-cells proliferate in response to Il-2 alone
• dramatically reduced numbers of B cells in the spleen
• IFN gamma levels in serum are increased

endocrine/exocrine glands
• numbers begin to decrease within a few days of birth




Genotype
MGI:3051904
ht2
Allelic
Composition
Socs1tm1Jni/Socs1+
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Socs1tm1Jni mutation (0 available); any Socs1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 50% of homozygotes die within 3 weeks of dimethylnitrosamine (DMN) while 90% of wild-type controls survive

neoplasm
• increase in liver tumors induced by diethylnitrosamine
• more of an increase in males than in females
• hyperplastic nodules with mild or no dysplasia

immune system
• increased TGF beta production
• plasma levels of various cytokines are increased
• IFN gamma levels increased
• levels are increased

liver/biliary system
• increased succeptibility to liver fibrosis due to diet or dimethylnitrosamine (DMN)
• liver damage is more severe
• increase in liver tumors induced by diethylnitrosamine
• more of an increase in males than in females
• hyperplastic nodules with mild or no dysplasia

homeostasis/metabolism
• plasma levels of various cytokines are increased
• IFN gamma levels increased
• increased TGF beta production
• levels are increased
• 50% of homozygotes die within 3 weeks of dimethylnitrosamine (DMN) while 90% of wild-type controls survive




Genotype
MGI:3783715
cx3
Allelic
Composition
Ifngtm1Ts/Ifngtm1Ts
Socs1tm1Jni/Socs1tm1Jni
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ifngtm1Ts mutation (18 available); any Ifng mutation (47 available)
Socs1tm1Jni mutation (0 available); any Socs1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• following culturing of IL-17 producing T cells in vitro, IL-17 production is twice as high as in similarly treated wild-type cells





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory